The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Littmann Electronic Stethoscope, Model 3200.
| Device ID | K083903 |
| 510k Number | K083903 |
| Device Name: | 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200 |
| Classification | Stethoscope, Electronic |
| Applicant | 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55144 -1000 |
| Contact | Jizhong Jin |
| Correspondent | Jizhong Jin 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55144 -1000 |
| Product Code | DQD |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-12-29 |
| Decision Date | 2009-07-15 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50707387770414 | K083903 | 000 |
| 50707387765526 | K083903 | 000 |
| 50707387765519 | K083903 | 000 |
| 50707387765502 | K083903 | 000 |
| 50707387765441 | K083903 | 000 |
| 50707387765434 | K083903 | 000 |
| 50707387765427 | K083903 | 000 |